Cargando…

Correction to: Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2021
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483532/ https://www.ncbi.nlm.nih.gov/pubmed/34008414 http://dx.doi.org/10.1161/JAHA.121.020840

Ejemplares similares

Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study
por: Ware, Stephanie M., et al.
Publicado: (2021)

Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy
por: Dries, Annika M., et al.
Publicado: (2021)

Correction: Pigs with δ-sarcoglycan deficiency exhibit traits of genetic cardiomyopathy
por: Matsunari, Hitomi, et al.
Publicado: (2020)

Correction: Calreticulin Induces Dilated Cardiomyopathy
por: Lee, Dukgyu, et al.
Publicado: (2013)

Correction: Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients
por: García-Vielma, Catalina, et al.
Publicado: (2023)

Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy
por: Esslinger, Ulrike, et al.
Publicado: (2020)

Correction: A Case Report of Takotsubo Cardiomyopathy With Myxedema Coma
por: Marin, Andrea C, et al.
Publicado: (2023)

Correction: Diuretic dose trajectories in dilated cardiomyopathy: prognostic implications
por: Nuzzi, Vincenzo, et al.
Publicado: (2022)

Correction: Cardiomyocyte-Specific Ablation of Med1 Subunit of the Mediator Complex Causes Lethal Dilated Cardiomyopathy in Mice
por: Jia, Yuzhi, et al.
Publicado: (2016)

Correction: Modulation of Serotonin Transporter Function during Fetal Development Causes Dilated Heart Cardiomyopathy and Lifelong Behavioral Abnormalities
por: Noorlander, Cornelle W., et al.
Publicado: (2009)

Correction to: Selenium supplementation in patients with peripartum cardiomyopathy: a proof‑of‑concept trial
por: Karaye, Kamilu M., et al.
Publicado: (2021)

Correction: reproducibility of in-vivo diffusion tensor cardiovascular magnetic resonance in hypertrophic cardiomyopathy
por: McGill, Laura-Ann, et al.
Publicado: (2013)

Correction: Taurine deficiency and dilated cardiomyopathy in golden retrievers fed commercial diets
por: Kaplan, Joanna L., et al.
Publicado: (2018)

Correction: Systematic review and meta-analysis of prolactin and iron deficiency in peripartum cardiomyopathy
Publicado: (2020)

Elevated Heart Rate and Survival in Children With Dilated Cardiomyopathy: A Multicenter Study From the Pediatric Cardiomyopathy Registry
por: Rossano, Joseph W., et al.
Publicado: (2020)

Correction: Clinical profile and prognostic factors of alcoholic cardiomyopathy in tribal and non-tribal population
Publicado: (2020)

Correction to: Cardiogenic shock secondary to stress-induced cardiomyopathy precipitated by severe diabetic ketoacidosis
Publicado: (2023)

Correction to: The year in cardiovascular medicine 2022: the top 10 papers in heart failure and cardiomyopathies
Publicado: (2023)

Correction: Laser-Supported CD133+ Cell Therapy in Patients with Ischemic Cardiomyopathy: Initial Results from a Prospective Phase I Multicenter Trial
Publicado: (2014)

Publisher Correction: Identification of key immune-related genes in dilated cardiomyopathy using bioinformatics analysis
por: Li, Feng, et al.
Publicado: (2023)

Correction to: Integrative analysis of genes reveals endoplasmic reticulum stress-related immune responses involved in dilated cardiomyopathy with fibrosis
por: Li, Wanpeng, et al.
Publicado: (2023)

Pediatric Restrictive Cardiomyopathies
por: Ditaranto, Raffaello, et al.
Publicado: (2022)

The Multifaced Perspectives of Genetic Testing in Pediatric Cardiomyopathies and Channelopathies
por: Popa-Fotea, Nicoleta-Monica, et al.
Publicado: (2020)

The phenotypic and genetic features of arrhythmogenic cardiomyopathy in the pediatric population
por: Kofeynikova, Olga, et al.
Publicado: (2023)

Correction: Establishment of a Novel Murine Model of Ischemic Cardiomyopathy with Multiple Diffuse Coronary Lesions
por: Nakaoka, Hajime, et al.
Publicado: (2013)

Correction: Reversal of Ischemic Cardiomyopathy with Sca-1(+) Stem Cells Modified with Multiple Growth Factors
por: Li, Ning, et al.
Publicado: (2020)

Correction: Osimertinib-induced biventricular cardiomyopathy with abnormal cardiac MRI findings: a case report
por: Patel, Karishma, et al.
Publicado: (2023)

Correction to: Psoriasis as risk factor for non-ischemic dilated cardiomyopathy: a population-based cross-sectional study
por: Alshami, Abbas, et al.
Publicado: (2021)

Correction to: Investigating changes in β‑adrenergic gene expression (ADRB1 and ADRB2) in Takotsubo (stress) cardiomyopathy syndrome; a pilot study
por: Onrat, Serap Tutgun, et al.
Publicado: (2022)

Cardiomyopathies in children
por: Hong, Young Mi
Publicado: (2013)

Correction: Biomarkers in Trypanosoma cruzi-Infected and Uninfected Individuals with Varying Severity of Cardiomyopathy in Santa Cruz, Bolivia
Publicado: (2014)

Correction: A Randomized, Double-Blind Trial of Lisinopril and Losartan for the Treatment of Cardiomyopathy in Duchenne Muscular Dystrophy
Publicado: (2015)

Correction to: Clinical Potential of Targeting Fibroblast Growth Factor‐23 and αKlotho in the Treatment of Uremic Cardiomyopathy
Publicado: (2020)

Correction: Approaches for monitoring and treating cardiomyopathy among cancer survivors following anthracycline or thoracic radiation treatment
por: Delavar, Arash, et al.
Publicado: (2022)

Correction to: Risk Score for Predicting 2‐Year Mortality in Patients With Chagas Cardiomyopathy From Endemic Areas: SaMi‐Trop Cohort Study
Publicado: (2021)

Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative Approach
por: Cimiotti, Diana, et al.
Publicado: (2021)

Correction: Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy
Publicado: (2018)

ICD Outcome in Pediatric Cardiomyopathies
por: Silvetti, Massimo Stefano, et al.
Publicado: (2022)

Correction: Structure-Based Analysis of A19D, a Variant of Transthyretin Involved in Familial Amyloid Cardiomyopathy
por: Ferreira, Priscila, et al.
Publicado: (2013)

Correction: Toll-Like Receptor (TLR) 2 and TLR4 Differentially Regulate Doxorubicin Induced Cardiomyopathy in Mice
por: Ma, Yonggang, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_dg73k1mkbpjl0afogo0sbhfhhh